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Local Trial Manager II

ICON Strategic Solutions

United States

Remote

USD 80,000 - 110,000

Full time

8 days ago

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Job summary

ICON Strategic Solutions is seeking a Local Trial Manager II for a fully remote role. The ideal candidate will manage global trials, ensuring effective execution and coordination with cross-functional teams. Candidates should have significant experience in clinical trial management and hold a bachelor's degree. This position offers a competitive salary and benefits, including medical and vision insurance, and a 401(k).

Benefits

Medical Insurance
Vision Insurance
401(k)

Qualifications

  • Minimum 3 years managing local, regional, or global trials in CRO, pharmaceutical, or biotech settings.
  • Bachelor's degree with 5+ years of relevant experience.

Responsibilities

  • Manage US portion of global trials, coordinating with cross-functional teams.
  • Plan and oversee clinical study execution aligned with global strategies.
  • Lead training for CRA, Investigators, and Study Coordinators.

Skills

Clinical Trial Management
Project Management
Communication

Education

Bachelor's Degree

Job description

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Direct message the job poster from ICON Strategic Solutions.

ICON has opened a new position for a Local Trial Manager II.

This is a fully remote role, with no travel required. Please apply to receive pay details.

Must currently work for a CRO, pharmaceutical, or biotechnology company, hold a bachelor’s degree, and have at least 5 years of clinical and 3 years of trial management experience. Relevant titles include Clinical Trial Manager, Local Trial Manager, Study Manager, Study Lead, Operations Manager, etc.

Responsibilities:
  1. Manage the US portion of global trials, coordinating with cross-functional teams, overseeing budgets, and vendors.
  2. Plan, manage, and oversee clinical study execution aligned with global strategies, leading the Local Study Team (LST).
  3. Support country-level operational planning and site selection within assigned countries.
  4. Develop program/study-specific materials such as monitoring plans and training documents.
  5. Participate in Clinical Study Teams (CSTs) / Trial Management Teams (TMTs), leading meetings as needed.
  6. Communicate country status, timelines, and deliverables to stakeholders, ensuring updates are reflected in relevant systems.
  7. Set goals and deliverables for clinical sites at the country level.
  8. Lead training for CRA, Investigators, and Study Coordinators.
  9. Oversee vendor activities, laboratories, and equipment provisioning.
  10. Engage with local teams and functions, including Medical Affairs and DFM.
  11. Contribute to the Country Operational Plan (COP) and collaborate with DFM and GCMs on feasibility and local delivery.
  12. Approve Baseline and Revised Enrolment Plans at the country level.
  13. Support study-level forecasting for investigational products and manage enrolment estimates.
Qualifications:
  • Minimum 3 years’ experience managing local, regional, or global trials in CRO, pharmaceutical, or biotech settings.
  • Bachelor’s degree with 5+ years of relevant experience.
Additional Details:
  • Seniority level: Associate
  • Employment type: Full-time
  • Job function: Research
  • Industry: Pharmaceutical Manufacturing

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Benefits:

Medical insurance, Vision insurance, 401(k).

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